Hemifacial Microsomia: Types, Symptoms & Treatment - Cleveland Clinic
Hemifacial microsomia occurs when one side of the face doesn’t develop as it should. It can affect your child’s ability to eat, see, hear, breathe and more. But they can still live a long, productive life. Surgery is often necessary to repair physical differences and maximize functioning.
Hemifacial microsomia - Wikipedia
Hemifacial microsomia (HFM) is a congenital disorder that affects the development of the lower half of the face, most commonly the ears, the mouth and the mandible. It usually occurs on one side of the face, but both sides are sometimes affected.
Hemifacial Microsomia | National Institute of Dental and …
Hemifacial microsomia is a condition in which one side of the face is smaller or underdeveloped or has parts that are missing. While the hallmark is unevenness (asymmetry) of the face, one or both sides may be affected.
Hemifacial Microsomia: Causes, Symptoms, and Treatments
2022年11月18日 · Hemifacial microsomia is the second most common birth defect, after cleft lip. Microsomia causes the structures of the face such as the jaw, cheek, lips, and skull to appear malformed.
Hemifacial Microsomia - StatPearls - NCBI Bookshelf
2023年8月8日 · Hemifacial microsomia (HFM), also known as unilateral otomandibular dysostosis or lateral facial dysplasia, is an asymmetrical, congenital malformation of the 1st and 2nd branchial arches and the second most common craniofacial anomaly after cleft lip and palate. [1]
Hemifacial Microsomia - Children's Hospital of Philadelphia
Hemifacial microsomia is a congenital condition in which the tissues on one side of the face are underdeveloped. It primarily affects the ear, mouth, and jaw areas, though it may also involve the eye, cheek, neck, and other parts of the skull, as well as nerves and soft tissue.
Hemifacial Microsomia - Johns Hopkins Medicine
What is hemifacial microsomia? Hemifacial microsomia is a common congenital facial difference that causes asymmetric development of the face. Hemifacial has been called many terms such as Goldenhar syndrome and oculo-auriculo-vertebral spectrum. They are all the same condition.
Hemifacial Microsomia - Boston Children's Hospital
Hemifacial microsomia (HFM), also called craniofacial microsomia or sometimes "Goldenhar syndrome," is a condition in which half of one side of the face is underdeveloped and does not grow normally. “Hemifacial” means one side of the face. “Microsomia” means smallness.
Craniofacial microsomia - MedlinePlus
Craniofacial microsomia is a term used to describe a spectrum of abnormalities that primarily affect the development of the skull (cranium) and face before birth. Explore symptoms, inheritance, genetics of this condition.
Hemifacial Microsomia (HFM) in Children
Hemifacial microsomia (HFM) is a congenital disorder. This means that your child is born with it. In this condition, one side of your baby’s face is underdeveloped (hemi means half). HFM usually only affects one side of the face. Sometimes both sides may be affected.
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